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枕颞骨纤维发育不良。病例报告。

Fibrous dysplasia of occipital and temporal bone. A case report.

作者信息

Neromyliotis Eleftherios, Sapountzi Marilia, Nikas Ioannis, Karydakis Ploutarchos, Mitsios Andreas, Sfakianos George, Themistocleous Marios S

机构信息

Department of Neurosurgery, Children's Hospital 'Agia Sofia', Athens, Greece.

ENT Department, Children's Hospital 'Agia Sofia', Athens, Greece.

出版信息

Oxf Med Case Reports. 2019 May 31;2019(5):omz039. doi: 10.1093/omcr/omz039. eCollection 2019 May.

DOI:10.1093/omcr/omz039
PMID:31198575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6544426/
Abstract

Fibrous dysplasia is a rare non-malignant condition where fibrous tissue replaces the normal bone architecture. Involvement of temporal and occipital bones is exceptionally rare and is associated with unique complications. A 10-year-old boy presented with right retroauricular enlargement and pain. Imaging studies and biopsy revealed fibrous dysplasia of the temporal and occipital bones. There was no hearing loss or sequelae arising from posterior fossa compression. The patient was discharged with follow-up instructions. Only 10 cases of occipital bone fibrous dysplasia have been reported in the medical literature. Occipital bone fibrous dysplasia can be complicated with Chiari malformation and syringomyelia while temporal bone involvement is associated with hearing loss. These potential developments require close follow-up that includes detailed neurologic examination, imaging and audiology.

摘要

骨纤维异常增殖症是一种罕见的非恶性疾病,其中纤维组织取代了正常的骨骼结构。颞骨和枕骨受累极为罕见,且伴有独特的并发症。一名10岁男孩出现右耳后肿大和疼痛。影像学检查和活检显示颞骨和枕骨骨纤维异常增殖症。没有因后颅窝受压导致的听力丧失或后遗症。患者出院时带有随访指示。医学文献中仅报道了10例枕骨骨纤维异常增殖症病例。枕骨骨纤维异常增殖症可并发Chiari畸形和脊髓空洞症,而颞骨受累与听力丧失有关。这些潜在的病情发展需要密切随访,包括详细的神经系统检查、影像学检查和听力检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5389/6544426/8ca1fd16381f/omz039f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5389/6544426/8ca1fd16381f/omz039f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5389/6544426/8ca1fd16381f/omz039f1.jpg

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本文引用的文献

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Chiari I Malformation and Basilar Invagination in Fibrous Dysplasia: Prevalence, Mechanisms, and Clinical Implications.纤维发育不良中的 Chiari I 畸形和颅底凹陷症:患病率、发病机制及临床意义。
J Bone Miner Res. 2018 Nov;33(11):1990-1998. doi: 10.1002/jbmr.3531. Epub 2018 Aug 3.
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Different clinical presentation and management of temporal bone fibrous dysplasia in children.儿童颞骨纤维结构不良的不同临床表现和治疗方法。
World J Surg Oncol. 2018 Jan 15;16(1):5. doi: 10.1186/s12957-017-1302-5.
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Association of Hearing Loss and Otologic Outcomes With Fibrous Dysplasia.
原发性颈静脉孔纤维发育不良:经硬膜外颞下经颈静脉入路的手术细节视频。病例展示
J Neurosurg Case Lessons. 2024 Oct 14;8(16). doi: 10.3171/CASE24396.
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A Rare Case of a Primary Leiomyoma of the Clivus in an Immunocompetent Patient and a Review of the Literature Regarding Clival Lesions.免疫功能正常患者中斜坡原发性平滑肌瘤的罕见病例及关于斜坡病变的文献综述
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Cranioplasty after Two Giant Intraosseous Angiolipomas of the Cranium: Case Report and Literature Review.颅骨两处巨大骨内血管脂肪瘤后的颅骨成形术:病例报告及文献综述
Healthcare (Basel). 2022 Mar 31;10(4):655. doi: 10.3390/healthcare10040655.
听力损失和耳科学结果与纤维发育不良的关系。
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